Skip to main content
Log in

Intermittent clamping is superior to ischemic preconditioning and its effect is more marked with shorter clamping cycles in the rat liver

  • Original Article—Liver, Pancreas, and Biliary Tract
  • Published:
Journal of Gastroenterology Aims and scope Submit manuscript

Abstract

Background

Intermittent clamping (IC) and ischemic preconditioning (PC) reportedly protect the liver against the ischemia/reperfusion (I/R) injury induced by inflow occlusion during hepatectomy. While IC cycles consisting of 15 min of clamping with 5 min of reperfusion are used empirically, the optimal IC cycle has not been established. We compared the effects of various cycles of IC and PC in the rat liver.

Methods

Rats subjected to 60 min of inflow occlusion were assigned to the following five groups (n = 8 each): 60 min of continuous ischemia; 4 cycles comprising 15 min of ischemia/5 min of reperfusion; 6 cycles comprising 10 min of ischemia/3.3 min of reperfusion; 12 cycles comprising 5 min of ischemia/1.7 min of reperfusion (the time ratio of ischemia to reperfusion in the IC groups was 3:1); and PC (10/10 min of ischemia/reperfusion) prior to 60 min of ischemia. The severity of liver injury was assessed by determining the serum alanine aminotransferase (ALT) level, bile flow, tissue glutathione content, and induction of apoptosis (terminal deoxynucleotidyl transferase-mediated biotin nick end-labeling [TUNEL] staining and DNA laddering), and by histological examination of areas of severe necrosis.

Results

All the parameters indicated that liver injury was attenuated in the three IC groups compared with the continuous group; furthermore, this effect became increasingly marked with shorter cycles of IC. PC did not exert a protective effect under the present experimental conditions.

Conclusion

Various cycles of IC consistently conferred protection against I/R injury, and IC with shorter cycles of ischemia and reperfusion was more effective. No protective effect of PC was evident. IC is a more robust strategy than the PC protocol for liver protection.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Subscribe and save

Springer+ Basic
$34.99 /Month
  • Get 10 units per month
  • Download Article/Chapter or eBook
  • 1 Unit = 1 Article or 1 Chapter
  • Cancel anytime
Subscribe now

Buy Now

Price includes VAT (Canada)

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6
Fig. 7
Fig. 8
Fig. 9

Similar content being viewed by others

References

  1. Kooby DA, Stockman J, Ben-Porat L, Gonen M, Jarnagin WR, Dematteo RP, et al. Influence of transfusions on perioperative and long-term outcome in patients following hepatic resection for colorectal metastases. Ann Surg. 2003;237:860–9.

    PubMed  Google Scholar 

  2. Tsao JI, Loftus JP, Nagomey DM, Adson MA, Ilstrup DM. Trends in morbidity and mortality of hepatic resection for malignancy: a matched comparative analysis. Ann Surg. 1994;220:199–205.

    Article  PubMed  CAS  Google Scholar 

  3. Pringle J. Note on the arrest of hepatic hemorrhage due to trauma. Ann Surg. 1908;48:501.

    Article  Google Scholar 

  4. Makuuchi M, Mori T, Gunven P, Yamazaki S, Hasegawa H. Safety of hemihepatic vascular occlusion during resection of the liver. Surg Gynecol Obstet. 1987;164:155–8.

    PubMed  CAS  Google Scholar 

  5. Imamura H, Seyama Y, Kokudo N, Maema A, Sugawara Y, Sano K, et al. One thousand fifty-six hepatectomies without mortality in 8 years. Arch Surg. 2003;138:1198–206.

    Article  PubMed  Google Scholar 

  6. Man K, Fan ST, Ng IO, Lo CM, Liu CL, Wong J. Prospective evaluation of Pringle maneuver in hepatectomy for liver tumors by a randomized study. Ann Surg. 1997;226:704–13.

    Article  PubMed  CAS  Google Scholar 

  7. Kim YI, Nakashima K, Tada I, Kawano K, Kobayashi M. Prolonged normothermic ischaemia of human cirrhotic liver during hepatectomy: a preliminary report. Br J Surg. 1993;80:1566–70.

    Article  PubMed  CAS  Google Scholar 

  8. Rudiger HA, Kang KJ, Sindram D, Riehle HM, Clavien PA. Comparison of ischemic preconditioning and intermittent and continuous inflow occlusion in the murine liver. Ann Surg. 2002;235:400–7.

    Article  PubMed  Google Scholar 

  9. Camargo CA Jr, Madden JF, Gao W, Selvan RS, Clavien PA. Interleukin-6 protects liver against warm ischemia/reperfusion injury and promotes hepatocyte proliferation in therodent. Hepatology. 1997;26:1513–20.

    Google Scholar 

  10. Belghiti J, Noun R, Malafosse R, Jagot P, Sauvanet A, Pierangeli F, et al. Continuous versus intermittent portal triad clamping for liver resection: a controlled study. Ann Surg. 1999;229:369–75.

    Article  PubMed  CAS  Google Scholar 

  11. Clavien PA, Selzner M, Rudiger HA, Graf R, Kadry Z, Rousson V, et al. A prospective randomized study in 100 consecutive patients undergoing major liver resection with versus without ischemic preconditioning. Ann Surg. 2003;238:843–52.

    Article  PubMed  Google Scholar 

  12. Petrowsky H, McCormack L, Trujillo M, Selzner M, Jochum W, Clavien PA. A prospective, randomized, controlled trial comparing intermittent portal triad clamping versus ischemic preconditioning with continuous clamping for major liver resection. Ann Surg. 2006;244:921–30.

    Article  PubMed  Google Scholar 

  13. Smymiotis V, Theodoraki K, Arkadopoulos N, Fragulidis G, Condi-Pafiti A, Plemenou-Fragou M, et al. Ischemic preconditioning versus intermittent vascular occlusion in liver resections performed under selective vascular exclusion: a prospective randomized study. Am J Surg. 2006;192:669–74.

    Article  Google Scholar 

  14. Peralta C, Closa D, Hotter G, Gelpí E, Prats N, Roselló-Catafau J. Liver ischemic preconditioning is mediated by the inhibitory action of nitric oxide on endothelin. Biochem Biopyhs Res Commun. 1996;22:264–70.

    Article  Google Scholar 

  15. Peralta C, Hotter G, Closa D, Gelpí E, Roselló-Catafau J. Protective effect of preconditioning on the injury associated to hepatic ischemia–reperfusion in the rat: role of nitric oxide and adenosine. Hepatology. 1997;30:1223–31.

    Google Scholar 

  16. Hardy KJ, Tancheroen S, Syulkes A. Comparison of continuous versus intermittent ischemia–reperfusion during liver resection in an experimental model. Br J Surg. 1995;82:833–6.

    Article  PubMed  CAS  Google Scholar 

  17. Isozaki H, Adam R, Gigou M, Szekely AM, Shen M, Bismuth H. Experimental study of the protective effect of intermittent hepatic pedicle clamping in the rat. Br J Surg. 1992;79:310–3.

    Article  PubMed  CAS  Google Scholar 

  18. van Wagensveld BA, van Gulik TM, Gelderblom HC, Scheepers JJ, Bosma A, Endert E, et al. Prolonged continuous or intermittent vascular inflow occlusion during hemihepatectomy in pigs. Ann Surg. 1999;229:376–84.

    Article  PubMed  Google Scholar 

  19. Nieuwenhuijs VB, de Bruijin MT, Schiesser M, Morphett A, Padbury RT, Barritt GJ. Ischemic preconditioning and intermittent ischemia preserve bile flow in a rat model of ischemia/reperfusion injury. Dig Dis Sci. 2007;52:3029–37.

    Article  PubMed  Google Scholar 

  20. Jang JH, Kang KJ, Kang Y, Lee IS, Graf R, Clavien PA. Ischemic preconditioning and intermittent clamping confer protection against ischemic injury in the cirrhotic mouse liver. Liver Transpl. 2008;14:980–8.

    Article  PubMed  Google Scholar 

  21. Horiuchi T, Muraoka R, Tabo T, Uchinami M, Kimura N, Tanigawa N. Optimal cycles of hepatic ischemia and reperfusion for intermittent pedicle clamping during liver surgery. Arch Surg. 1995;130:754–8.

    Article  PubMed  CAS  Google Scholar 

  22. Miyagawa Y, Imamura H, Soeda J, Matsunaga K, Mochida S, Fujiwara K, et al. Fate of hepatocyte and sinusoidal lining cell function and kinetics after extended cold preservation and transplantation of the rat liver. Liver Transpl. 2002;8:370–81.

    Article  PubMed  Google Scholar 

  23. Peralta C, Closa D, Xaus C, Gelpi E, Rosello-Catafau J, Hotter G. Hepatic preconditioning in rats is defined by a balance of adenosine and xanthine. Hepatology. 1998;28:768–73.

    Article  PubMed  CAS  Google Scholar 

  24. Bowers BA, Branum GD, Rotolo FS, Watters CR, Meyers WC. Bile flow—an index of ischemic injury. J Surg Res. 1987;42:565–9.

    Article  PubMed  CAS  Google Scholar 

  25. Koeppel TA, Trauner M, Mennone A, Arrese M, Rios-Velez L, Boyer JL. Role of glutathione in hepatic bile formation during reperfusion after cold ischemia of the rat liver. J Hepatol. 1998;28:812–9.

    Article  PubMed  CAS  Google Scholar 

  26. Jaeschke H. Molecular mechanisms of hepatic ischemia–reperfusion injury and preconditioning. Am J Physiol Gastrointest Liver Physiol. 2003;284:G15–26.

    PubMed  CAS  Google Scholar 

  27. Liu P, Fisher MA, Farhood A, Smith CW, Jaeschke H. Beneficial effects of extracellular glutathione against endotoxin-induced liver injury during ischemia and reperfusion. Circ Shock. 1994;43:64–70.

    PubMed  CAS  Google Scholar 

  28. Dunne JB, Davenport M, Williams R, Tredger JM. Evidence that S-adenosylmethionine and N-acetylcysteine reduce injury from sequential cold and warm ischemia in the isolated perfused rat liver. Transplantation. 1994;57:1161–7.

    Article  PubMed  CAS  Google Scholar 

  29. Kobayashi H, Kurokawa T, Kitahara S, Nonami T, Harada A, Nakao A, et al. The effects of gamma-glutamylcysteine ethyl ester, a prodrug of glutathione, on ischemia–reperfusion-induced liver injury in rats. Transplantation. 1992;54:414–8.

    Article  PubMed  CAS  Google Scholar 

  30. Serafin A, Rosello-Catafau J, Prats N, Xaus C, Gelpi E, Peralta C. Ischemic preconditioning increase the tolerance of fatty liver to hepatic ischemia–reperfusion injury in the rat. Am J Pathol. 2002;161:587–601.

    Article  PubMed  Google Scholar 

  31. Amersi F, Nelson SK, Shen XD, Kato H, Melinek J, Kupiec-Weglinski JW, et al. Bucillamine, a thiol antioxidant, prevents transplantation-associated reperfusion injury. Proc Natl Acad Sci USA. 2002;99:8915–20.

    Article  PubMed  CAS  Google Scholar 

  32. Schauer RJ, Gerbes AL, Vonier D, op den Winkel M, Fraunberger P, Bilzer M. Induction of cellular resistance against Kupffer cell-derived oxidant stress: a novel concept of hepatoprotection by ischemic preconditioning. Hepatology. 2003;37:286–295.

    Google Scholar 

  33. Accatino L, Pizarro M, Solís N, Arrese M, Koenig CS. Bile secretory function after warm hepatic ischemia–reperfusion injury in the rat. Liver Transpl. 2003;9:1199–210.

    Article  PubMed  Google Scholar 

  34. Lawson JA, Fisher MA, Simmons CA, Farhood A, Jaeschke H. Parenchymal cell apoptosis as a signal for sinusoidal sequestration and transendothelial migration of neutrophils in murine models endotoxin- and Fas-antibody-mediated liver injury. Hepatology. 1998;28:761–7.

    Article  PubMed  CAS  Google Scholar 

  35. Jaeschke H, Fisher MA, Lawson JA, Simmons CA, Farhood A, Jones DA. Activation of caspase-3 (CPP32)-like proteases is essential for TNF-a-induced hepatic parenchymal cell apoptosis and neutrophil-mediated necrosis in a murine endotoxin shock model. J Immunol. 1998;160:3480–6.

    PubMed  CAS  Google Scholar 

  36. Gujral JS, Bucci TJ, Farhood A, Jaeschke H. Mechanism of cell death during warm hepatic ischemia–reperfusion in rats: apoptosis or necrosis? Hepatology. 2001;33:397–405.

    Article  PubMed  CAS  Google Scholar 

  37. Cursio R, Gugenheim J, Ricci JE, Crenesse D, Rostagno P, Maulon L, et al. A caspase inhibitor fully protects rats against lethal normothermic liver ischemia by inhibition of liver apoptosis. FASEB J. 1999;13:253–61.

    PubMed  CAS  Google Scholar 

  38. Sindram D, Porte RJ, Hoffman MR, Bentley RC, Clavien PA. Platelets induce sinusoidal endothelial cell apoptosis upon reperfusion of the cold ischemic rat liver. Gastroenterology. 2000;118:183–91.

    Article  PubMed  CAS  Google Scholar 

  39. Kang KJ, Jang JH, Lim TJ, Kang Y, Park KK, Lee IS, et al. Optimal cycle of intermittent portal triad clamping during liver resection in the murine liver. Liver Transpl. 2004;10:794–801.

    Article  PubMed  Google Scholar 

  40. Kobayashi A, Imamura H, Isobe M, Matsuyama Y, Soeda J, Matsunaga K, et al. Mac-1(CD11b/CD18) and intercellular adhesion molecule-1 in ischemia–reperfusion injury of rat liver. Am J Physiol Gastrointest Liver Physiol. 2001;281:G577–85.

    PubMed  CAS  Google Scholar 

  41. Jaeschke H, Lemasters JJ. Apoptosis versus oncotic necrosis in hepatic ischemia/reperfusion injury. Gastroenterology. 2003;125:1246–57.

    Article  PubMed  CAS  Google Scholar 

  42. Schmidt-Nielsen K. Scaling: why is animal size so important? Cambridge: Cambridge University Press; 1984. p. 241.

    Book  Google Scholar 

Download references

Acknowledgments

This work was supported by a Grant-in-Aid for Scientific Research (B) (20390352) from Ministry of Education, Culture, Sports, Science and Technology and by Mitsui Life Social Welfare Foundation.

Conflict of interest

The authors do not have a financial relationship with any organization that sponsored the research. The authors also have full control of all primary data and that they agree to allow the journal to review their data if requested.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Hiroshi Imamura.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Seyama, Y., Imamura, H., Inagaki, Y. et al. Intermittent clamping is superior to ischemic preconditioning and its effect is more marked with shorter clamping cycles in the rat liver. J Gastroenterol 48, 115–124 (2013). https://doi.org/10.1007/s00535-012-0613-0

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00535-012-0613-0

Keywords

Navigation